Division of Genomics of Development and Disease, Institute for Molecular Bioscience, The University of Queensland, St Lucia, Brisbane, QLD 4073, Australia.
Division of Cell Biology and Molecular Medicine, Institute for Molecular Bioscience, The University of Queensland, St Lucia, Brisbane, QLD 4073, Australia.
Dev Cell. 2019 Apr 22;49(2):279-292.e5. doi: 10.1016/j.devcel.2019.03.017.
The correct assignment of cell fate within fields of multipotent progenitors is essential for accurate tissue diversification. The first lymphatic vessels arise from pre-existing veins after venous endothelial cells become specified as lymphatic progenitors. Prox1 specifies lymphatic fate and labels these progenitors; however, the mechanisms restricting Prox1 expression and limiting the progenitor pool remain unknown. We identified a zebrafish mutant that displayed premature, expanded, and prolonged lymphatic specification. The gene responsible encodes the regulator of alternative splicing, Nova2. In zebrafish and human endothelial cells, Nova2 selectively regulates pre-mRNA splicing for components of signaling pathways and phosphoproteins. Nova2-deficient endothelial cells display increased Mapk/Erk signaling, and Prox1 expression is dynamically controlled by Erk signaling. We identify a mechanism whereby Nova2-regulated splicing constrains Erk signaling, thus limiting lymphatic progenitor cell specification. This identifies the capacity of a factor that tunes mRNA splicing to control assignment of cell fate during vascular differentiation.
在多能祖细胞的领域中正确分配细胞命运对于准确的组织多样化至关重要。最初的淋巴管是在静脉内皮细胞被特化为淋巴管祖细胞后从现有的静脉中出现的。Prox1 指定淋巴管命运并标记这些祖细胞;然而,限制 Prox1 表达并限制祖细胞库的机制仍然未知。我们鉴定了一种表现出过早、扩大和延长的淋巴管特化的斑马鱼突变体。负责该基因的编码是选择性剪接调节剂 Nova2。在斑马鱼和人类内皮细胞中,Nova2 选择性地调节信号通路和磷酸蛋白成分的前体 mRNA 剪接。Nova2 缺陷型内皮细胞显示出增加的 Mapk/Erk 信号,而 Prox1 的表达受 Erk 信号的动态控制。我们确定了一种机制,其中 Nova2 调节的剪接限制了 Erk 信号,从而限制了淋巴管祖细胞的特化。这确定了一个因素的能力,即调节 mRNA 剪接,以控制血管分化过程中的细胞命运分配。